1. Crystal Structure of Group II Chaperonin in the Open State
Yanwu Huo, Zhongjun Hu, Kai Zhang, Li Wang, Yujia Zhai, Qiangjun Zhou, Gabe Lander, Jiang Zhu, Yongzhi He, Xiaoyun Pang, Wei Xu, Mark Bartlam, Zhiyang Dong, Fei Sun 
Structure 
Volume 18, Issue 10, Pages (October 2010)
DOI: /j.str
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2. Structure 2010 18, 1270-1279DOI: (10.1016/j.str.2010.07.009)
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3. Figure 1 Crystal Structure of rATcpnβ
(A) Structural features of the rATcpnβ monomer, colored by domain. The lid is purple, apical domain is red, intermediate domain is yellow, and the equatorial domain is green. The modeled ADP is colored by element.
(B) Topology of rATcpnβ monomer.
(C) The stereo view of nucleotide binding site of rATcpnβ. The 2Fo-Fc omit difference map (contour level 0.8) shows an elongated stretch of electron density on top of the equatorial domain, into which the ADP could be modeled. The adjacent residues involved in interaction are labeled.
(D and E) Side and top views of overall rATcpnβ structure.
(F) Hydrophobic patch in the lid domain of group II chaperonin. Hydrophobic surface representation of rATcpnβ crystal structure. The hydrophobic surface is colored by yellow and the hydrophilic by blue.
(G) Sequence alignments of thermosomes across several species reveal hydrophobic patch in the lid is conserved and corresponding site is indicated in green triangle. The GenBank accessions of protein sequences form top to bottom are AAO47380, YP_255343, YP_ , NP_963436, YP_ , NP_275933, NP_142040, YP_ , ZP_ , ABX13688, and ACB08055, respectively.
See also Figure S1.
Structure  , DOI: ( /j.str )
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4. Figure 2
Comparison of the Monomer and Overall structures of the Two Thermosome States
(A) The rATcpnβ crystal structure is an open state colored in cyan. The TKcpn crystal structure represents the closed state colored in pink.
(B) Superposition of the overall structures for rATcpnβ in the open state (cyan) and closed state (pink) based on the cryoEM and nsEM map, respectively. One isolated subunit is enlarged and shown on the right. See also Figure S2 and Movies S1–S5.
Structure  , DOI: ( /j.str )
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5. Figure 3
CryoEM Structure of rATcpnβ in Open State and Atomic Structure Fitting
(A) Raw image of particles in cryo-EM. Top and side views are indicated by blue arrows. The scale bar is 50 nm.
(B) Averaging views (top, tilt, and side) of selected 2D classes of cryoEM particles of rATcpnβ_ATP are matched to the corresponding 3D projections. The top view exhibiting 10-fold symmetry, with a small portion (∼10%) from 2D classification indicated in the blue square.
(C) Surface representation of the side, inner, top, and bottom views of the cryo-EM structure of rATcpnβ_ATP. The cryo-EM structure of rATcpnβ_apo is similar to rATcpnβ_ATP and not shown here. EM map are colored based on domain division, with the apical and lid domains in cyan, the intermediate domain in yellow, and the equatorial domain in red.
(D) Equatorial, apical domain, and side views of the rATcpnβ subunit crystal structure fit into the rATcpnβ_ATP cryoEM map.
See also Figures S3–S5.
Structure  , DOI: ( /j.str )
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6. Figure 4
Negative Staining EM Structure of rATcpnβ in Closed State and Atomic Structure Fitting
(A) Raw EM image of negatively stained particles. Top and side views are indicated by blue arrows. The scale bar is 50nm.
(B) Averaging views (top, tilt, and side) of selected 2D classes of the negatively stained particles are matched to the corresponded 3D projections.
(C) Surface representation of the side, inner, top, and bottom views of the negative stain structure. EM map are colored based on domain division, with the apical and lid domains in cyan, the intermediate domain in yellow, and the equatorial domain in red.
(D) Side, top, and bottom views of the TKcpn subunit crystal structure fit into the rATcpnβ nsEM map.
See also Figures S4–S5.
Structure  , DOI: ( /j.str )
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7. Figure 5
ATP Binding without Hydrolysis Could Not Trigger a Closed Structure for Group II Chaperonin
(A) A comparison of the electron density near the ATP-binding sites of the rATcpnβ_apo and rATcpnβ_ATP cryoEM maps. On the left the rATcpnβ crystal structure is fitted into the rATcpnβ_ATP cryoEM map. The middle shows the difference map between the rATcpnβ_ATP cryoEM map and the rATcpnβ crystal structure with ADP omitted. The right shows the rATcpnβ crystal structure is fitted into the rATcpnβ_apo cryoEM map. ATP shown as red stick model is placed into the nucleotide binding pocket.
(B) Protease K digestion assay of rATcpnβ under different conditions. The rATcpnβ incubated with ADP, ATP, ADP/NaF/AlCl3, or ATP/NaF/AlCl3 were digested by protease K at 65°C for 5 min. Each lane is labeled.
Structure  , DOI: ( /j.str )
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